A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3472291



Internal ID18718212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16884145..16920575hg38UCSC Ensembl
Innerchr1:17210640..17247070hg19UCSC Ensembl
Innerchr1:17083227..17119657hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3836431
hg1936431
hg1836431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011411
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3472291
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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